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Spirodiclofen

Spirodiclofen is an acaricide and insecticide used in agriculture to control mites and San Jose scale. In the United States, it is used on citrus, grapes, pome fruit, stone fruit, and tree nut crops.[1][2]

Spirodiclofen
Names
Preferred IUPAC name
3-(2,4-Dichlorophenyl)-2-oxo-1-oxaspiro[4.5]non-3-en-4-yl 2,2-dimethylbutanoate
Identifiers
  • 148477-71-8 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:38639
ChEMBL
  • ChEMBL2227839
ChemSpider
  • 17215909
ECHA InfoCard 100.130.204
EC Number
  • 604-636-5
KEGG
  • C18553
  • 177863
UNII
  • 3X7G31F5MX Y
  • DTXSID6034928
  • InChI=1S/C21H24Cl2O4/c1-4-20(2,3)19(25)26-17-16(13-10-14(22)12-15(23)11-13)18(24)27-21(17)8-6-5-7-9-21/h10-12H,4-9H2,1-3H3
    Key: OYNVHVAEOLJJPV-UHFFFAOYSA-N
  • CCC(C)(C)C(=O)OC1=C(C(=O)OC12CCCCC2)c3cc(cc(c3)Cl)Cl
Properties
C21H24Cl2O4
Molar mass 411.32 g·mol−1
Appearance White solid
Melting point 94.8 °C (202.6 °F; 367.9 K)[1]
Hazards
GHS labelling:
Danger
H317, H350, H361, H373, H410
P201, P202, P260, P261, P272, P273, P280, P281, P302+P352, P308+P313, P314, P321, P333+P313, P363, P391, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Spirodiclofen belongs to the tetronic acid class and acts by inhibiting lipid biosynthesis.[3]

References edit

  1. ^ a b "EPA Pesticide Fact Sheet: Spirodiclofen" (PDF). Environmental Protection Agency.
  2. ^ "Spirodiclofen" (PDF). Food and Agricultural Organization of the United Nations.
  3. ^ De Maeyer, L; Geerinck, R (2009). "The multiple target use of spirodiclofen (Envidor 240 SC) in IPM pomefruit in Belgium". Communications in Agricultural and Applied Biological Sciences. 74 (1): 225–32. PMID 20218531.

spirodiclofen, acaricide, insecticide, used, agriculture, control, mites, jose, scale, united, states, used, citrus, grapes, pome, fruit, stone, fruit, tree, crops, names, preferred, iupac, name, dichlorophenyl, oxaspiro, dimethylbutanoate, identifiers, number. Spirodiclofen is an acaricide and insecticide used in agriculture to control mites and San Jose scale In the United States it is used on citrus grapes pome fruit stone fruit and tree nut crops 1 2 Spirodiclofen Names Preferred IUPAC name 3 2 4 Dichlorophenyl 2 oxo 1 oxaspiro 4 5 non 3 en 4 yl 2 2 dimethylbutanoate Identifiers CAS Number 148477 71 8 Y 3D model JSmol Interactive image ChEBI CHEBI 38639 ChEMBL ChEMBL2227839 ChemSpider 17215909 ECHA InfoCard 100 130 204 EC Number 604 636 5 KEGG C18553 PubChem CID 177863 UNII 3X7G31F5MX Y CompTox Dashboard EPA DTXSID6034928 InChI InChI 1S C21H24Cl2O4 c1 4 20 2 3 19 25 26 17 16 13 10 14 22 12 15 23 11 13 18 24 27 21 17 8 6 5 7 9 21 h10 12H 4 9H2 1 3H3Key OYNVHVAEOLJJPV UHFFFAOYSA N SMILES CCC C C C O OC1 C C O OC12CCCCC2 c3cc cc c3 Cl Cl Properties Chemical formula C 21H 24Cl 2O 4 Molar mass 411 32 g mol 1 Appearance White solid Melting point 94 8 C 202 6 F 367 9 K 1 Hazards GHS labelling Pictograms Signal word Danger Hazard statements H317 H350 H361 H373 H410 Precautionary statements P201 P202 P260 P261 P272 P273 P280 P281 P302 P352 P308 P313 P314 P321 P333 P313 P363 P391 P405 P501 Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Infobox references Spirodiclofen belongs to the tetronic acid class and acts by inhibiting lipid biosynthesis 3 References edit a b EPA Pesticide Fact Sheet Spirodiclofen PDF Environmental Protection Agency Spirodiclofen PDF Food and Agricultural Organization of the United Nations De Maeyer L Geerinck R 2009 The multiple target use of spirodiclofen Envidor 240 SC in IPM pomefruit in Belgium Communications in Agricultural and Applied Biological Sciences 74 1 225 32 PMID 20218531 Retrieved from https en wikipedia org w index php title Spirodiclofen amp oldid 1139824095, wikipedia, wiki, book, books, library,

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